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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097915copy number variation1nstd102humanPathogenic GRCh37 chr9: 101,867,488-101,867,604 , GRCh38.p12 chr9: 99,105,206-99,105,322 TGFBR1
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7072100inversion1nstd229human GRCh38 chr9: 99,102,541-99,102,587 , GRCh37.p13 chr9: 101,864,823-101,864,869 TGFBR1
    nsv7068550inversion1nstd229human GRCh38 chr9: 99,145,334-99,145,419 , GRCh37.p13 chr9: 101,907,616-101,907,701 TGFBR1, RNA5SP290
    nsv6877183copy number variation1nstd229human GRCh38 chr9: 99,126,701-99,215,200 , GRCh37.p13 chr9: 101,888,983-101,977,482 RN7SL794P, LOC105376174, 3 more genes
    nsv6873654copy number variation1nstd229human GRCh38 chr9: 99,135,333-99,137,310 , GRCh37.p13 chr9: 101,897,615-101,899,592 TGFBR1
    nsv6871305copy number variation1nstd229human GRCh38 chr9: 99,150,916-99,151,640 , GRCh37.p13 chr9: 101,913,198-101,913,922 TGFBR1
    nsv6866893copy number variation1nstd229human GRCh38 chr9: 99,123,923-99,124,127 , GRCh37.p13 chr9: 101,886,205-101,886,409 TGFBR1
    nsv6859496copy number variation1nstd229human GRCh38 chr9: 99,097,032-99,102,520 , GRCh37.p13 chr9: 101,859,314-101,864,802 TGFBR1
    nsv6858919copy number variation1nstd229human GRCh38 chr9: 98,942,817-99,140,966 , GRCh37.p13 chr9: 101,705,099-101,903,248 COL15A1, TGFBR1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6447795copy number variation1nstd223human GRCh38 chr9: 99,103,501-99,106,300 , GRCh37.p13 chr9: 101,865,783-101,868,582 TGFBR1
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    nsv6447695copy number variation1nstd223human GRCh38 chr9: 99,145,617-99,146,188 , GRCh37.p13 chr9: 101,907,899-101,908,470 TGFBR1, RNA5SP290
    nsv6439392copy number variation1nstd223human GRCh38 chr9: 99,128,640-99,128,950 , GRCh37.p13 chr9: 101,890,922-101,891,232 TGFBR1
    nsv6437582copy number variation1nstd223human GRCh38 chr9: 99,130,793-99,131,308 , GRCh37.p13 chr9: 101,893,075-101,893,590 TGFBR1
    nsv6436237copy number variation1nstd223human GRCh38 chr9: 99,097,032-99,102,517 , GRCh37.p13 chr9: 101,859,314-101,864,799 TGFBR1
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
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